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Merck

FAM58A

family with sequence similarity 58, member A

동의어:
STAR
:
UniProtKB ID:
Clone ID:
  • Human(92002) Summary: Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]
  • domestic cat(101087461) family with sequence similarity 58, member A
  • dog(492239) family with sequence similarity 58, member A
  • cow(534796) family with sequence similarity 58, member A
  • domestic guinea pig(100728930) family with sequence similarity 58, member A
  • Zebrafish(553650) family with sequence similarity 58, member A
  • sheep(101111859) family with sequence similarity 58, member A

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Antibodies

제품 번호
설명
종별 반응성
응용분야
Anti-FAM58A antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution,
종별 반응성
human
응용분야
immunohistochemistry
Anti-FAM58A antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody,
종별 반응성
human
응용분야
immunofluorescence

esiRNA

제품 번호
설명
MISSION® esiRNA, targeting human FAM58A,
human